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Enantiomeric fraction evaluation of pharmaceuticals in environmentalmatrices by liquid chromatography-tandem mass spectrometry

dc.contributor.authorRibeiro, Ana Rita
dc.contributor.authorSantos, Lúcia
dc.contributor.authorMaia, Alexandra S.
dc.contributor.authorDelerue-Matos, Cristina
dc.contributor.authorCastro, Paula M.L.
dc.contributor.authorTiritan, Maria Elizabeth
dc.date.accessioned2015-01-06T16:24:25Z
dc.date.available2015-01-06T16:24:25Z
dc.date.issued2014-10-10
dc.description.abstractThe interest for environmental fate assessment of chiral pharmaceuticals is increasing and enantioselective analytical methods are mandatory. This study presents an enantioselective analytical method for the quantification of seven pairs of enantiomers of pharmaceuticals and a pair of a metabolite. The selected chiral pharmaceuticals belong to three different therapeutic classes, namely selective serotonin reuptake inhibitors (venlafaxine, fluoxetine and its metabolite norfluoxetine), beta-blockers (alprenolol, bisoprolol, metoprolol, propranolol) and a beta2-adrenergic agonist (salbutamol). The analytical method was based on solid phase extraction followed by liquid chromatography tandem mass spectrometry with a triple quadrupole analyser. Briefly, Oasis® MCX cartridges were used to preconcentrate 250 mL of water samples and the reconstituted extracts were analysed with a Chirobiotic™ V under reversed mode. The effluent of a laboratory-scale aerobic granular sludge sequencing batch reactor (AGS-SBR) was used to validate the method. Linearity (r2 > 0.99), selectivity and sensitivity were achieved in the range of 20–400 ng L−1 for all enantiomers, except for norfluoxetine enantiomers which range covered 30–400 ng L−1. The method detection limits were between 0.65 and 11.5 ng L−1 and the method quantification limits were between 1.98 and 19.7 ng L−1. The identity of all enantiomers was confirmed using two MS/MS transitions and its ion ratios, according to European Commission Decision 2002/657/EC. This method was successfully applied to evaluate effluents of wastewater treatment plants (WWTP) in Portugal. Venlafaxine and fluoxetine were quantified as non-racemic mixtures (enantiomeric fraction ≠ 0.5). The enantioselective validated method was able to monitor chiral pharmaceuticals in WWTP effluents and has potential to assess the enantioselective biodegradation in bioreactors. Further application in environmental matrices as surface and estuarine waters can be exploited.por
dc.identifier.doi10.1016/j.chroma.2014.06.099
dc.identifier.urihttp://hdl.handle.net/10400.22/5322
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.relation.ispartofseriesJournal of Chromatography A;Vol. 1363
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S0021967314010449por
dc.subjectLC-MS/MSpor
dc.subjectChiral pharmaceuticalspor
dc.subjectEnantiomeric fractionpor
dc.subjectMacrocyclic antibiotic CSPpor
dc.subjectChirobiotic Vpor
dc.titleEnantiomeric fraction evaluation of pharmaceuticals in environmentalmatrices by liquid chromatography-tandem mass spectrometrypor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage235por
oaire.citation.startPage226por
oaire.citation.titleJournal of Chromatography Apor
oaire.citation.volume1363por
person.familyNameDelerue-Matos
person.givenNameCristina
person.identifier.ciencia-id9A1A-43FB-5C27
person.identifier.orcid0000-0002-3924-776X
person.identifier.ridD-4990-2013
person.identifier.scopus-author-id6603741848
rcaap.rightsopenAccesspor
rcaap.typearticlepor
relation.isAuthorOfPublication09f6a7bd-2f15-42b0-adc5-04bd22210519
relation.isAuthorOfPublication.latestForDiscovery09f6a7bd-2f15-42b0-adc5-04bd22210519

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